EP2410053B2 - Antisense-verbindungen - Google Patents
Antisense-verbindungen Download PDFInfo
- Publication number
- EP2410053B2 EP2410053B2 EP11186113.4A EP11186113A EP2410053B2 EP 2410053 B2 EP2410053 B2 EP 2410053B2 EP 11186113 A EP11186113 A EP 11186113A EP 2410053 B2 EP2410053 B2 EP 2410053B2
- Authority
- EP
- European Patent Office
- Prior art keywords
- wing
- nucleoside
- antisense
- modified
- bna
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/111—General methods applicable to biologically active non-coding nucleic acids
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- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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- C12N2310/11—Antisense
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- C12N2310/3231—Chemical structure of the sugar modified ring structure having an additional ring, e.g. LNA, ENA
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- C12N2310/33—Chemical structure of the base
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- C12N2310/00—Structure or type of the nucleic acid
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- C12N2310/34—Spatial arrangement of the modifications
- C12N2310/341—Gapmers, i.e. of the type ===---===
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- C12N2310/351—Conjugate
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- C12N2320/00—Applications; Uses
- C12N2320/50—Methods for regulating/modulating their activity
- C12N2320/53—Methods for regulating/modulating their activity reducing unwanted side-effects
Definitions
- Targeting disease-causing gene sequences was first suggested nearly 40 years ago ( Belikova et al., Tet. Lett., 1967, 37, 3557-3562 ), and antisense activity was demonstrated in cell culture a decade later ( Zamecnik et al., Proc. Natl. Acad. Sci. U.S.A., 1978, 75, 280-284 ).
- One advantage of antisense technology in the treatment of a disease or condition that stems from a disease-causing gene is that it is a direct genetic approach that has the ability to modulate expression of specific disease-causing genes.
- Another advantage is that validation of a target using antisense compounds results in direct and immediate discovery of the therapeutic agent.
- RNAi RNA interference
- RNAi is a form of antisense-mediated gene silencing involving the introduction of dsRNA leading to the sequence-specific reduction of targeted endogenous mRNA levels. This sequence-specificity makes antisense compounds extremely attractive as tools for target validation and gene functionalization, as well as therapeutics to selectively modulate the expression of genes involved in the pathogenesis of any one of a variety of diseases.
- Antisense technology is an effective means for reducing the expression of one or more specific gene products and can therefore prove to be uniquely useful in a number of therapeutic, diagnostic, and research applications.
- Chemically modified nucleosides are routinely used for incorporation into antisense compounds to enhance one or more properties, such as nuclease resistance, pharmacokinetics or affinity for a target RNA.
- BNA bicyclic nucleic acid
- gapmer antisense compounds for inhibition of target RNA in vivo comprising high-affinity bicyclic nucleotide modifications, but which are designed to have mitigated toxicity by incorporation of non-bicyclic high-affinity modified nucleotides.
- Such gapmer antisense compounds are more effective than previously described BNA or LNA antisense compounds, as a result of a reduction in toxicity.
- Fluiter et al. discloses locked nucleic acid monomers and various oligonucleotides that include such monomers in symmetric gapmers.
- a gapmer antisense oligonucleotide comprising a deoxy gap region, a 5' wing region positioned at the 5' end of the deoxy gap, and a 3' wing region positioned at the 3' end of the deoxy gap, wherein at least one nucleoside of at least one of the wing regions is a 4' to 2' bicyclic nucleoside and at least one of the remaining wing nucleosides is a non-bicyclic 2'-O(CH2) 2 OCH 3 modified nucleoside, and wherein the deoxy gap region is between 7 and 10 nucleosides in length, and the wing regions are between 1 to 7 nucleosides in length, and the oligomeric compound having at least one modified internucleoside linkage.
- gapmer antisense oligonucleotides which exhibit marked improvements in safety as compared to a gapmer of the same length and wing-gap-wing configuration, wherein each wing nucleotide is a bicyclic nucleic acid (BNA), for example a methyleneoxy (4'-CH 2 -O-2') BNA, sometimes also referred to as LNA.
- BNA bicyclic nucleic acid
- the gapmer antisense oligonucleotides have at least one LNA nucleotide (methyleneoxy (4'-CH 2 -O-2') BNA) or ethyleneoxy (4'-CH 2 CH 2 -O-2') BNA in at least one of the wings and at least non-bicyclic high-affinity modified nucleotide.
- gapmer antisense oligonucleotides having a deoxy gap, a 5' wing region positioned at the 5' end of the deoxy gap, and a 3' wing region positioned at the 3' end of the deoxy gap, wherein the 5' wing region has at least one non-bicyclic high-affinity modified nucleotide and the 3' wing region has at least one 4' to 2' bicyclic nucleotide, for example a LNA nucleotide (methyleneoxy (4'-CH 2 -O-2') BNA) or an ethyleneoxy (4'-CH 2 CH 2 -O-2') BNA.
- LNA nucleotide methyleneoxy (4'-CH 2 -O-2'
- BNA ethyleneoxy (4'-CH 2 CH 2 -O-2'
- the non-bicyclic high-affinity modified nucleotides are non-bicyclic 2'-modified nucleosides, specifically the non-bicyclic 2'-modified nucleosides are 2'-O(CH 2 ) 2 OCH 3 .
- the gapmer antisense oligonucleotides have no BNAs in the 5' wing region, for example no LNA nucleosides (methyleneoxy (4'-CH 2 -O-2') BNAs) or ethyleneoxy (4'-CH 2 CH 2 -O-2') BNAs.
- the gapmer antisense oligonucleotides disclosed herein have a 5' wing region having only 2'-O(CH 2 ) 2 OCH 3 modified nucleotides and only LNA nucleosides (methyleneoxy (4'-CH 2 -O-2') BNAs) or ethyleneoxy (4'-CH 2 CH 2 -O-2') BNAs in the 3' wing.
- the gapmer antisense oligonucleotides wherein the 5' region has at least one 4' to 2' bicyclic nucleotide and the 3' wing region has at least one non-bicyclic 2'-modified nucleotide.
- the gapmer antisense oligonucleotides have no LNA nucleotides in the 3' wing region, for example no LNA nucleotides (methyleneoxy (4'-CH 2 -O-2') BNAs) or ethyleneoxy (4'-CH 2 CH 2 -O-2') BNAs.
- the gapmer antisense oligonucleotides disclosed herein have a 5' wing region having only BNA nucleotides, for example only LNA nucleotides (methyleneoxy (4'-CH 2 -O-2') BNAs) or ethyleneoxy (4'-CH 2 CH 2 -O-2') BNAs, and a 3' wing region having only 2'-modified nucleosides.
- the non-bicyclic 2'-modified nucleosides are 2'-O(CH 2 ) 2 OCH 3 .
- the gapmer antisense oligonucleotides of the present invention can be shortmers, provided they fall within the scope of the appended claims.
- the gapmer antisense oligonucleotides are 10 to 30, 10 to 14, 12 to 25, 15 to 25, or 18 to 24 nucleotides in length.
- the 5' and 3' wing regions of the antisense compounds of the present invention are independently between 1 and 7 nucleotides in length, or 1, 2, 3, 4, 5, 6 or 7 nucleotides in length; between 1 and 5 nucleotides in length, or 1, 2, 3, 4, or 5 nucleotides in length; or between 1 to 3 nucleotides in length, or 1, 2, or 3 nucleotides in length.
- the deoxy gap region of the antisense oligonucleotides of the present invention are between 7 and 10 nucleotides in length, or 7, 8, 9, or 10 nucleotides in length.
- the gapmer antisense oligonucleotides have a wing-gap-wing configuration of 5-10-5, 3-10-3, 2-10-2, 1-10-1 or 2-8-2.
- the gapmer antisense oligonucleotides delineated herein have at least one modified internucleoside linkage.
- this modified internucleoside linkage is a phosphorothioate.
- each internucleoside linkage is a phosphorothioate modified internucleoside linkage.
- the high-affinity modified nucleotides are sugar-modified nucleotides.
- at least one of the sugar-modified nucleotides comprises a bridge between the 4' and the 2' position of the sugar.
- Each of the sugar-modified nucleotides is, independently, ⁇ -D or ⁇ -L.
- each of said high-affinity modified nucleotides confers a ⁇ T m of at least 1 to 4 degrees per nucleotide.
- each of said sugar-modified nucleotides comprises a 2'-substituent group that is other than H or OH.
- Such sugar-modified nucleotides include those having a 4' to 2' bridged bicyclic nucleotide.
- each of the sugar-modified nucleotides is a non-bicyclic 2'-substituent groups, which are independently, alkoxy, substituted alkoxy, substituted or unsubstituted -O-(2-acetylamide) or halogen.
- each of the 2'-substituent groups is OCH 2 CH 2 OCH 3 .
- each of said bridges is, independently, -[C(R 1 )(R 2 ) n- , -[C(R 1 )(R 2 )] n -O-, -C(R 1 R 2 )-N(R 1 )-O- or -C(R 1 R 2 )-O-N(R 1 )-.
- each of said bridges is, independently, 4'-(CH 2 ) 2 -2', 4'-(CH 2 ) 2 -2', 4'-CH 2 -O-2', 4'-(CH 2 ) 2 -O-2', 4'-CH 2 -O-N(R 1 )-2' and 4'-CH 2 -N(R 1 )-O-2'- wherein each R 1 is, independently, H, a protecting group or C 1 -C 12 alkyl.
- gapmer antisense compounds with one or more 2'-modified or 2'-substituted nucleosides.
- the term "2'-modified nucleoside” or “2'-substituted nucleoside” as used in the present invention is intended to include all manner of nucleosides having a 2'-substituent group that is other than H and OH.
- These 2'-substituent groups can be further substituted with substituent groups selected from hydroxyl, amino, alkoxy, carboxy, benzyl, phenyl, nitro (NO 2 ), thiol, thioalkoxy (S-alkyl), halogen, alkyl, aryl, alkenyl and alkynyl where each R m is, independently, H, an amino protecting group or substituted or unsubstituted C 1 -C 10 alkyl.
- gapmer antisense compounds for use in therapy. Further provided is a gapmer antisense compound of the present invention for use in inhibiting expression of a target RNA in an animal.
- natural nucleoside or “unmodified nucleoside” means a nucleoside comprising a natural nucleobase and a natural sugar. Natural nucleosides include RNA and DNA nucleosides.
- natural sugar refers to a sugar of a nucleoside that is unmodified from its naturally occurring form in RNA (2'-OH) or DNA (2'-H).
- nucleotide refers to a nucleoside having a phosphate group covalently linked to the sugar. Nucleotides may be modified with any of a variety of substituents.
- nucleobase refers to the base portion of a nucleoside or nucleotide.
- a nucleobase may comprise any atom or group of atoms capable of hydrogen bonding to a base of another nucleic acid.
- nucleobase refers to a nucleobase that is unmodified from its naturally occurring form in RNA or DNA.
- heterocyclic base moiety refers to a nucleobase comprising a heterocycle.
- oligomeric compound refers to a polymeric structure comprising two or more substructures and capable of hybridizing to a region of a nucleic acid molecule.
- oligomeric compounds are oligonucleosides.
- oligomeric compounds are oligonucleotides.
- oligomeric compounds are antisense compounds.
- oligomeric compounds are antisense oligonucleotides.
- oligomeric compounds comprise conjugate groups.
- Nonlimiting examples of oligomeric compounds include, but are not limited to, primers, probes, antisense compounds, antisense oligonucleotides, external guide sequence (EGS) oligonucleotides, alternate splicers, and siRNAs. As such, these compounds can be introduced in the form of single-stranded, double-stranded, circular, branched or hairpins and can contain structural elements such as internal or terminal bulges or loops. Oligomeric double-stranded compounds can be two strands hybridized to form double-stranded compounds or a single strand with sufficient self complementarity to allow for hybridization and formation of a fully or partially double-stranded compound.
- oligonucleoside refers to an oligonucleotide in which the internucleoside linkages do not contain a phosphorus atom.
- oligonucleotide refers to an oligomeric compound comprising a plurality of linked nucleotides or nucleosides.
- one or more nucleotides of an oligonucleotide is modified.
- an oligonucleotide comprises ribonucleic acid (RNA) or deoxyribonucleic acid (DNA).
- oligonucleotides are composed of natural and/or modified nucleobases, sugars and covalent internucleoside linkages, and may further include non-nucleic acid conjugates.
- nucleoside linkage refers to a covalent linkage between adjacent nucleosides.
- natural internucleotide linkage refers to a 3' to 5' phosphodiester linkage.
- modified internculeoside linkage refers to any linkage between nucleosides or nucleotides other than a naturally occuring internucleoside linkage.
- antisense compound refers to an oligomeric compound that is at least partially complementary to a target nucleic acid molecule to which it hybridizes. In certain embodiments, an antisense compound modulates (increases or decreases) expression of a target nucleic acid.
- Antisense compounds include, but are not limited to, compounds that are oligonucleotides, oligonucleosides, oligonucleotide analogs, oligonucleotide mimetics, and chimeric combinations of these. Consequently, while all antisense compounds are oligomeric compounds, not all oligomeric compounds are antisense compounds.
- antisense oligonucleotide refers to an antisense compound that is an oligonucleotide.
- antisense activity refers to any detectable and/or measurable activity attributable to the hybridization of an antisense compound to its target nucleic acid. Such detection and or measuring may be direct or indirect. For example, in certain embodiments, antisense activity is assessed by detecting and or measuring the amount of target protein. In certain embodiments, antisense activity is assessed by detecting and/or measuring the amount of target nucleic acids and/or cleaved target nucleic acids and/or alternatively spliced target nucleic acids.
- detecting antisense activity or “measuring antisense activity” means that a test for detecting or measuring antisense activity is performed on a sample and compared to that of a control sample. Such detection and/or measuring may include values of zero. Thus, if a test for detection of antisense activity results in a finding of no antisense activity (antisense activity of zero), the step of "detecting antisense activity" has nevertheless been performed.
- control sample refers to a sample that has not been contacted with a test compound.
- a control sample is obtained prior to administration of an oligomeric compound to an animal.
- a control sample is obtained from an animal to which oligomeric compound is not administered.
- a reference standard is used as a surrogate for a control sample.
- chimeric antisense compound refers to an antisense compound, having at least one sugar, nucleobase and/or internucleoside linkage that is differentially modified as compared to the other sugars, nucleobases and internucleoside linkages within the same oligomeric compound. The remainder of the sugars, nucleobases and internucleoside linkages can be independently modified or unmodified.
- a chimeric oligomeric compound will have modified nucleosides that can be in isolated positions or grouped together in regions that will define a particular motif. Any combination of modifications and or mimetic groups can comprise a chimeric oligomeric compound as described herein.
- motif' refers to a pattern of unmodified and modified nucleotides or linkages in an oligomeric compound.
- mixed-backbone antisense oligonucleotide refers to an antisense oligonucleotide wherein at least one internucleoside linkage of the antisense oligonucleotide is different from at least one other internucleotide linkage of the antisense oligonucleotide.
- target protein refers to a protein, the modulation of which is desired.
- target gene refers to a gene encoding a target.
- target nucleic acid refers to any nucleic acid molecule, the amount or function of which is capable of being modulated by an antisense compound.
- Target nucleic acids include, but are not limited to, RNA (including, but not limited to pre-mRNA and mRNA or portions thereof), cDNA derived from such RNA, as well as non-translated RNA, such as miRNA.
- a target nucleic acid can be a cellular gene (or mRNA transcribed from such gene) whose expression is associated with a particular disorder or disease state, or a nucleic acid molecule from an infectious agent.
- target region refers to a portion of a target nucleic acid which, is capable of hybridizing one or more antisense compound and such hybridization results in antisense activity.
- target segment refers to a shorter sub-portions of a target region
- target site refers to a portion of a target nucleic acid that is capable of hybridizing with an antisense compound, resulting in antisense activity.
- targeting refers to the association of an antisense compound to a particular target nucleic acid molecule or a particular region of nucleotides within a target nucleic acid molecule.
- design or “designed to” refer to the process of designing an oligomeric compound that specifically hybridizes with a selected target nucleic acid molecule.
- nucleobase complementarity refers to a nucleobase that is capable of base pairing with another nucleobase.
- adenine (A) is complementary to thymine (T).
- adenine (A) is complementary to uracil (U).
- complementary nucleobase refers to a nucleobase of an antisense compound that is capable of base pairing with a nucleobase of its target nucleic acid.
- nucleobase at a certain position of an antisense compound is capable of hydrogen bonding with a nucleobase at a certain position of a target nucleic acid
- the position of hydrogen bonding between the oligonucleotide and the target nucleic acid is considered to be complementary at that nucleobase pair.
- non-complementary nucleobase refers to a pair of nucleobases that do not form hydrogen bonds with one another or otherwise support hybridization.
- the term "complementary” refers to the capacity of an oligomeric compound to hybridize to another oligomeric compound or nucleic acid through nucleobase complementarity.
- an antisense compound and its target are complementary to each other when a sufficient number of corresponding positions in each molecule are occupied by nucleobases that can bond with each other to allow stable association between the antisense compound and the target.
- nucleobases that can bond with each other to allow stable association between the antisense compound and the target.
- antisense compounds that may comprise up to about 20% nucleotides that are mismatched (i.e., are not nucleobase complementary to the corresponding nucleotides of the target).
- the antisense compounds contain no more than about 15%, more preferably not more than about 10%, most preferably not more than 5% or no mismatches.
- the remaining nucleotides are nucleobase complementary or otherwise do not disrupt hybridization (e.g., universal bases).
- One of ordinary skill in the art would recognize the compounds provided herein are at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% nucleobase complementary to a target nucleic acid.
- hybridization means the pairing of complementary oligomeric compounds (e.g., an antisense compound and its target nucleic acid). While not limited to a particular mechanism, the most common mechanism of pairing involves hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleoside or nucleotide bases (nucleobases).
- nucleobases complementary nucleoside or nucleotide bases
- the natural base adenine is nucleobase complementary to the natural nucleobases thymidine and uracil which pair through the formation of hydrogen bonds.
- the natural base guanine is nucleobase complementary to the natural bases cytosine and 5-methyl cytosine. Hybridization can occur under varying circumstances.
- the term “specifically hybridizes” refers to the ability of an oligomeric compound to hybridize to one nucleic acid site with greater affinity than it hybridizes to another nucleic acid site.
- an antisense oligonucleotide specifically hybridizes to more than one target site.
- an oligomeric compound specifically hybridizes with its target under stringent hybridization conditions.
- stringent hybridization conditions or “stringent conditions” refers to conditions under which an antisense compound will hybridize to its target sequence, but to a minimal number of other sequences. Stringent conditions are sequence-dependent and will be different in different circumstances, and “stringent conditions” under which antisense compounds hybridize to a target sequence are determined by the nature and composition of the antisense compounds and the assays in which they are being investigated.
- percent complementary refers to the number of nucleobases of an oligomeric compound that have nucleobase complementarity with a corresponding nucleobase of another oligomeric compound or nucleic acid divided by the total length (number of nucleobases) of the oligomeric compound.
- region of percent complementarity refers to the number of nucleobases of a region of an oligomeric compound that have nucleobase complementarity with a corresponding nucleobase of another oligomeric compound or nucleic acid divided by the total length (number of nucleobases) of the region.
- modulation refers to a perturbation of function or activity when compared to the level of the function or activity prior to modulation.
- modulation includes the change, either an increase (stimulation or induction) or a decrease (inhibition or reduction) in gene expression.
- modulation of expression can include perturbing splice site selection of pre-mRNA processing.
- expression refers to all the functions and steps by which a gene's coded information is converted into structures present and operating in a cell. Such structures include, but are not limited to the products of transcription and translation.
- variant refers to an alternative RNA transcript that can be produced from the same genomic region of DNA. Variants include, but are not limited to “pre-mRNA variants” which are transcripts produced from the same genomic DNA that differ from other transcripts produced from the same genomic DNA in either their start or stop position and contain both intronic and exonic sequence. Variants also include, but are not limited to, those with alternate splice junctions, or alternate initiation and termination codons.
- 2'-modified or “2'-substituted” means a sugar comprising substituent at the 2' position other than H or OH.
- MOE refers to a 2'-O-methoxyethyl substituent
- the term "gapmer” refers to a chimeric oligomeric compound comprising a central region (a "gap") and a region on either side of the central region (the “wings”), wherein the gap comprises at least one modification difference compared to each wing.
- modifications include nucleobase, monomeric linkage, and sugar modifications as well as the absence of modification (unmodified RNA or DNA).
- the nucleotide linkages in each of the wings are different than the nucleotide linkages in the gap.
- each wing comprises nucleotides with high affinity modifications and the gap comprises nucleotides that do not comprise that modification.
- nucleotides in the gap and the nucleotides in the wings all comprise high affinity modifications, but the high affinity modifications in the gap are different than the high affinity modifications in each of the wings.
- the modifications in the wings are the same as one another. In certain embodiments, the modifications in the wings are different from each other. In certain embodiments, nucleotides in the gap are unmodified and nucleotides in the wings are modified. In certain embodiments, the modification(s) within each wing are the same. In certain embodiments, the modification(s) in one wing are different from the modification(s) in the other wing.
- short antisense compound or “shortmer oligonucleotide” refers to a gapmer antisense compound or antisense oligonucleotide 10, 11, 12, 13 or 14 nucleotides in length having a deoxy gap 6 to 12 nucleotides in length having wing regions that are independently 1 to 4 high-affinity modified nucleotides in length.
- exemplary wing-deoxy gap-wing configurations are 4-6-4, 3-6-3, 2-6-2, 4-7-4, 3-7-3, 2-7-2, 4-8-4, 3-8-3, 2-8-2, 1-8-1, 2-9-2, 1-9-1, 2-10-2, 1-10-1, 1-12-1, and the like.
- a "gap-widened antisense oligonucleotide” refers to a chimeric antisense oligonucleotide with a deoxy gap region which is greater than 10 nucleotides in length having wing regions that are independently one to eight high-affinity modified nucleotides in length.
- the gap-widened antisense oligonucleotides are 18 to 24 nucleotides in length capable of having, for example, various wing-gap-wing motifs selected from: 1-16-1, 2-15-1, 1-15-2, 1-14-3, 3-14-1, 2-14-2, 1-13-4, 4-13-1, 2-13-3, 3-13-2, 1-12-5, 5-12-1, 2-12-4, 4-12-2, 3-12-3, 1-11-6, 6-11-1, 2-11-5, 5-11-2, 3-11-4, 4-11-3, 1-17-1, 2-16-1, 1-16-2, 1-15-3, 3-15-1, 2-15-2, 1-14-4, 4-14-1, 2-14-3, 3-14-2, 1-13-5, 5-13-1, 2-13-4, 4-13-2, 3-13-3, 1-12-6, 6-12-1, 2-12-5, 5-12-2, 3-12-4, 4-12-3, 1-11-7, 7-11-1, 2-11-6, 6-11-2, 3-11-5, 5-11-3, 4-11-4, 1-18-1, 1-17-2
- 6-12-2 3-12-5, 5-12-3, 4-12-4, 1-11-8, 8-11-1, 2-11-7, 7-11-2, 3-11-6, 6-11-3, 4-11-5, 5-11-4, 1-19-1, 1-18-2, 2-18-1, 1-17-3, 3-17-1, 2-17-2, 1-16-4, 4-16-1, 2-16-3, 3-16-2, 1-15-5, 2-15-4, 4-15-2, 3-15-3, 1-14-6, 6-14-1, 2-14-5, 5-14-2, 3-14-4, 4-14-3, 1-13-7, 7-13-1, 2-13-6, 6-13-2, 3-13-5, 5-13-3, 4-13-4, 1-12-8, 8-12-1, 2-12-7, 7-12-2, 3-12-6, 6-12-3, 4-12-5, 5-12-4, 2-11-8, 8-11-2, 3-11-7, 7-11-3, 4-11-6, 6-11-4, 5-11-5, 1-20-1, 1-19-2, 2-19-1, 1-18-3, 3-18-1, 2-18-2, 1-17-4, 4-17-1, 2-17-3, 3-17-2
- high-affinity modified nucleotide refers to a nucleotide having at least one modified nucleobase, internucleoside linkage or sugar moiety, such that the modification increases the affinity of an antisense compound comprising the modified nucleotide to a target nucleic acid.
- High-affinity modifications include, but are not limited to, BNAs, LNAs and 2'-MOE.
- mimetic refers to groups that are substituted for a sugar, a nucleobase, and/ or internucleoside linkage. Generally, a mimetic is used in place of the sugar or sugar-internucleoside linkage combination, and the nucleobase is maintained for hybridization to a selected target.
- Representative examples of a sugar mimetic include, but are not limited to, cyclohexenyl or morpholino.
- Representative examples of a mimetic for a sugar-internucleoside linkage combination include, but are not limited to, peptide nucleic acids (PNA) and morpholino groups linked by uncharged achiral linkages.
- PNA peptide nucleic acids
- nucleobase mimetics are well known in the art and include, but are not limited to, tricyclic phenoxazine analogs and universal bases (Berger et al., Nuc Acid Res. 2000, 28:2911-14). Methods of synthesis of sugar, nucleoside and nucleobase mimetics are well known to those skilled in the art.
- BNA bicyclic nucleoside
- the term "bicyclic nucleoside” or “BNA” refers to a nucleoside wherein the furanose portion of the nucleoside includes a bridge connecting two atoms on the furanose ring, thereby forming a bicyclic ring system.
- BNAs include, but are not limited to, ⁇ -L-LNA, ⁇ -D-LNA, ENA, Oxyamino BNA (2'-O-N(CH 3 )-CH 2 -4') and Aminooxy BNA (2'-N(CH 3 )-O-CH 2 -4').
- the term "4' to 2' bicyclic nucleoside” refers to a BNA wherin the bridge connecting two atoms of the furanose ring bridges the 4' carbon atom and the 2' carbon atom of the furanose ring, thereby forming a bicyclic ring system.
- BNA's include but are not limited to:
- a "locked nucleic acid” or “LNA” refers to a nucleotide modified such that the 2'-hydroxyl group of the ribosyl sugar ring is linked to the 4' carbon atom of the sugar ring via a methylene groups, thereby forming a 2'-C,4'-C-oxymethylene linkage.
- LNAs include, but are not limited to, ⁇ -L-LNA, and ⁇ -D-LNA.
- prodrug refers to a therapeutic agent that is prepared in an inactive form that is converted to an active form (i.e., drug) within the body or cells thereof by the action of endogenous enzymes or other chemicals and/or conditions.
- pharmaceutically acceptable salts refers to salts of active compounds that retain the desired biological activity of the active compound and do not impart undesired toxicological effects thereto.
- cap structure or “terminal cap moiety” refers to chemical modifications, which have been incorporated at either terminus of an antisense compound.
- prevention refers to delaying or forestalling the onset or development of a condition or disease for a period of time from hours to days, preferably weeks to months.
- the term “amelioration” refers to a lessening of at least one indicator of the severity of a condition or disease.
- the severity of indicators may be determined by subjective or objective measures which are known to those skilled in the art.
- treatment refers to administering a composition of the invention to effect an alteration or improvement of the disease or condition.
- Prevention, amelioration, and/or treatment may require administration of multiple doses at regular intervals, or prior to onset of the disease or condition to alter the course of the disease or condition.
- a single agent may be used in a single individual for each prevention, amelioration, and treatment of a condition or disease sequentially, or concurrently.
- the term "pharmaceutical agent” refers to a substance provides a therapeutic benefit when administered to a subject.
- terapéuticaally effective amount refers to an amount of a pharmaceutical agent that provides a therapeutic benefit to an animal.
- administering means providing a pharmaceutical agent to an animal, and includes, but is not limited to administering by a medical professional and self-administering.
- a pharmaceutical composition refers to a mixture of substances suitable for administering to an individual.
- a pharmaceutical composition may comprise an antisense oligonucleotide and a sterile aqueous solution.
- animal refers to a human or non-human animal, including, but not limited to, mice, rats, rabbits, dogs, cats, pigs, and non-human primates, including, but not limited to, monkeys and chimpanzees.
- parenteral administration refers to administration through injection or infusion.
- Parenteral administration includes, but is not limited to, subcutaneous administration, intravenous administration, or intramuscular administration.
- subcutaneous administration refers to administration just below the skin.
- Intravenous administration means administration into a vein.
- a dose refers to a specified quantity of a pharmaceutical agent provided in a single administration.
- a dose may be administered in two or more boluses, tablets, or injections.
- the desired dose requires a volume not easily accommodated by a single injection.
- two or more injections may be used to achieve the desired dose.
- a dose may be administered in two or more injections to minimize injection site reaction in an individual.
- a dosage unit refers to a form in which a pharmaceutical agent is provided.
- a dosage unit is a vial comprising lyophilized antisense oligonucleotide.
- a dosage unit is a vial comprising reconstituted antisense oligonucleotide.
- active pharmaceutical ingredient refers to the substance in a pharmaceutical composition that provides a desired effect.
- side effects refers to physiological responses attributable to a treatment other than desired effects.
- side effects include, without limitation, injection site reactions, liver function test abnormalities, renal function abnormalities, liver toxicity, renal toxicity, central nervous system abnormalities, and myopathies.
- increased aminotransferase levels in serum may indicate liver toxicity or liver function abnormality.
- increased bilirubin may indicate liver toxicity or liver function abnormality.
- therapeutic index refers to some measure of activity or potency divided by some measure of toxicity.
- alkyl refers to a saturated straight or branched hydrocarbon radical containing up to twenty four carbon atoms.
- alkyl groups include, but are not limited to, methyl, ethyl, propyl, butyl, isopropyl, n-hexyl, octyl, decyl, dodecyl and the like.
- Alkyl groups typically include from 1 to about 24 carbon atoms, more typically from 1 to about 12 carbon atoms (C 1 -C 12 alkyl) with from 1 to about 6 carbon atoms being more preferred.
- the term "lower alkyl” as used herein includes from 1 to about 6 carbon atoms.
- Alkyl groups as used herein may optionally include one or more further substituent groups.
- alkenyl refers to a straight or branched hydrocarbon chain radical containing up to twenty four carbon atoms and having at least one carbon-carbon double bond.
- alkenyl groups include, but are not limited to, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, dienes such as 1,3-butadiene and the like.
- Alkenyl groups typically include from 2 to about 24 carbon atoms, more typically from 2 to about 12 carbon atoms with from 2 to about 6 carbon atoms being more preferred.
- Alkenyl groups as used herein may optionally include one or more further substituent groups
- alkynyl refers to a straight or branched hydrocarbon radical containing up to twenty four carbon atoms and having at least one carbon-carbon triple bond.
- alkynyl groups include, but are not limited to, ethynyl, 1-propynyl, 1-butynyl, and the like.
- Alkynyl groups typically include from 2 to about 24 carbon atoms, more typically from 2 to about 12 carbon atoms with from 2 to about 6 carbon atoms being more preferred.
- Alkynyl groups as used herein may optionally include one or more further substitutent groups.
- aminoalkyl refers to an amino substituted alkyl radical. This term is meant to include C 1 -C 12 alkyl groups having an amino substituent at any position and wherein the alkyl group attaches the aminoalkyl group to the parent molecule. The alkyl and/or amino portions of the aminoalkyl group can be further substituted with substituent groups.
- aliphatic refers to a straight or branched hydrocarbon radical containing up to twenty four carbon atoms wherein the saturation between any two carbon atoms is a single, double or triple bond.
- An aliphatic group preferably contains from 1 to about 24 carbon atoms, more typically from 1 to about 12 carbon atoms with from 1 to about 6 carbon atoms being more preferred.
- the straight or branched chain of an aliphatic group may be interrupted with one or more heteroatoms that include nitrogen, oxygen, sulfur and phosphorus.
- Such aliphatic groups interrupted by heteroatoms include without limitation polyalkoxys, such as polyalkylene glycols, polyamines, and polyimines. Aliphatic groups as used herein may optionally include further substitutent groups.
- alicyclic refers to a cyclic ring system wherein the ring is aliphatic.
- the ring system can comprise one or more rings wherein at least one ring is aliphatic.
- Preferred alicyclics include rings having from about 5 to about 9 carbon atoms in the ring.
- Alicyclic as used herein may optionally include further substitutent groups.
- alkoxy refers to a radical formed between an alkyl group and an oxygen atom wherein the oxygen atom is used to attach the alkoxy group to a parent molecule.
- alkoxy groups include, but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, n-pentoxy, neopentoxy, n-hexoxy and the like.
- Alkoxy groups as used herein may optionally include further substitutent groups.
- aryl and “aromatic,” refer to a mono- or polycyclic carbocyclic ring system radicals having one or more aromatic rings.
- aryl groups include, but are not limited to, phenyl, naphthyl, tetrahydronaphthyl, indanyl, idenyl and the like.
- Preferred aryl ring systems have from about 5 to about 20 carbon atoms in one or more rings.
- Aryl groups as used herein may optionally include further substitutent groups.
- aralkyl and “arylalkyl,” refer to a radical formed between an alkyl group and an aryl group wherein the alkyl group is used to attach the aralkyl group to a parent molecule. Examples include, but are not limited to, benzyl, phenethyl and the like. Aralkyl groups as used herein may optionally include further substitutent groups attached to the alkyl, the aryl or both groups that form the radical group.
- heterocyclic radical refers to a radical mono-, or poly-cyclic ring system that includes at least one heteroatom and is unsaturated, partially saturated or fully saturated, thereby including heteroaryl groups. Heterocyclic is also meant to include fused ring systems wherein one or more of the fused rings contain at least one heteroatom and the other rings can contain one or more heteroatoms or optionally contain no heteroatoms.
- a heterocyclic group typically includes at least one atom selected from sulfur, nitrogen or oxygen.
- heterocyclic groups include, [1,3]dioxolane, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, quinoxalinyl, pyridazinonyl, tetrahydrofuryl and the like.
- Heterocyclic groups as used herein may optionally include further substitutent groups.
- heteroaryl refers to a radical comprising a mono- or poly-cyclic aromatic ring, ring system or fused ring system wherein at least one of the rings is aromatic and includes one or more heteroatom. Heteroaryl is also meant to include fused ring systems including systems where one or more of the fused rings contain no heteroatoms. Heteroaryl groups typically include one ring atom selected from sulfur, nitrogen or oxygen.
- heteroaryl groups include, but are not limited to, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzooxazolyl, quinoxalinyl, and the like.
- Heteroaryl radicals can be attached to a parent molecule directly or through a linking moiety such as an aliphatic group or hetero atom.
- Heteroaryl groups as used herein may optionally include further substitutent groups.
- heteroarylalkyl refers to a heteroaryl group as previously defined having an alky radical that can attach the heteroarylalkyl group to a parent molecule. Examples include, but are not limited to, pyridinylmethyl, pyrimidinylethyl, napthyridinylpropyl and the like. Heteroarylalkyl groups as used herein may optionally include further substitutent groups on one or both of the heteroaryl or alkyl portions.
- the term "mono or poly cyclic structure" includes all ring systems that are single or polycyclic having rings that are fused or linked and is meant to be inclusive of single and mixed ring systems individually selected from aliphatic, alicyclic, aryl, heteroaryl, aralkyl, arylalkyl, heterocyclic, heteroaryl, heteroaromatic, heteroarylalkyl.
- Such mono and poly cyclic structures can contain rings that are uniform or have varying degrees of saturation including fully saturated, partially saturated or fully unsaturated.
- Each ring can comprise ring atoms selected from C, N, O and S to give rise to heterocyclic rings as well as rings comprising only C ring atoms which can be present in a mixed motif such as for example benzimidazole wherein one ring has only carbon ring atoms and the fused ring has two nitrogen atoms.
- mono or poly cyclic structures can be attached to a parent molecule directly through a ring atom, through a substituent group or a bifunctional linking moiety.
- acyl refers to a radical formed by removal of a hydroxyl group from an organic acid an d has the general formula -C(O)-X where X is typically aliphatic, alicyclic or aromatic. Examples include aliphatic carbonyls, aromatic carbonyls, aliphatic sulfonyls, aromatic sulfinyls, aliphatic sulfinyls, aromatic phosphates, aliphatic phosphates and the like. Acyl groups as used herein may optionally include further substitutent groups.
- hydrocarbyl includes groups comprising C, O and H. Included are straight, branched and cyclic groups having any degree of saturation. Such hydrocarbyl groups can include one or more heteroatoms selected from N, O and S and can be further mono or poly substituted with one or more substituent groups.
- substituted and “substituent group,” include groups that are typically added to other groups or parent compounds to enhance desired properties or give desired effects. Substituent groups can be protected or unprotected and can be added to one available site or to many available sites in a parent compound. Substituent groups may also be further substituted with other substituent groups and may be attached directly or via a linking group such as an alkyl or hydrocarbyl group to a parent compound.
- each R aa , R bb and R cc is, independently, H, an optionally linked chemical functional group or a further substituent group with a preferred list including without limitation H, alkyl, alkenyl, alkynyl, aliphatic, alkoxy, acyl, aryl, aralkyl, heteroaryl, alicyclic,heterocyclic and heteroarylalkyl.
- chemical modifications improve the potency and/or efficacy of antisense compounds, improving the potential for oral delivery as well as enhancing subcutaneous administration, decreasing the potential for side effects, and leading to improvements in patient convenience.
- chemical modifications that increase the potency of antisense compounds allow administration of lower doses, which reduces the potential for toxicity, as well as decreasing overall cost of therapy.
- modifications that increase resistance to degradation result in slower clearance from the body, which in certain embodiments, allows for less frequent dosing.
- oligomeric compounds comprising certain chemical modifications or motifs are less toxic than other oligomeric compounds comprising different modifications and/or motifs. In certain embodiments, administration of such oligomeric compounds results in less hepatotoxicity. It is often preferable to include chemical modifications in oligonucleotides to alter their activity. Chemical modifications can alter oligonucleotide activity by, for example: increasing affinity of an antisense oligonucleotide for its target RNA, increasing nuclease resistance, and/or altering the pharmacokinetics of the oligonucleotide.
- the use of chemistries that increase the affinity of an oligonucleotide for its target can allow for the use of shorter oligonucleotide compounds.
- the invention provides oligomeric compounds that have favorable characteristics for in vivo administration.
- gapmer antisense compounds of the present invention have been designed. Certain such gapmer antisense compounds optionally can further comprise a conjugate group. Certain gapmer antisense compounds of the present invention are shortmers, provided they fall within the scope of the appended claims. Certain gapmer antisense compounds of the present disclosure are gap-widened antisense oligonucleotides.
- the present invention provides oligomeric compounds comprising oligonucleotides.
- Certain oligonuculeotides comprise 8 to 30 linked nucleosides.
- the oligomeric compounds comprise modified nucleosides, modified internucleoside linkages and/or conjugate groups.
- the compounds described herein contain one or more asymmetric centers and thus give rise to enantiomers, diastereomers, and other stereoisomeric configurations that may be defined, in terms of absolute stereochemistry, as (R) or (S), ⁇ or ⁇ , or as (D) or (L) such as for amino acids et al. Included in the antisense compounds provided herein are all such possible isomers, as well as their racemic and optically pure forms.
- the invention provides oligomeric compounds comprising linked nucleosides. In certain embodiments, some or all of the nucleosides are modified nucleosides. In certain embodiments, one or more nucleoside comprises a modified nucleobase. In certain embodiments, one or more nucleoside comprises a modified sugar.
- a nucleobase is any group that contains one or more atom or groups of atoms capable of hydrogen bonding to a base of another nucleic acid.
- nucleobases such as the purine nucleobases adenine (A) and guanine (G), and the pyrimidine nucleobases thymine (T), cytosine (C) and uracil (U)
- A purine nucleobase
- G guanine
- T cytosine
- U uracil
- modified nucleobase and nucleobase mimetic can overlap but generally a modified nucleobase refers to a nucleobase that is fairly similar in structure to the parent nucleobase, such as for example a 7-deaza purine, a 5-methyl cytosine, or a G-clamp, whereas a nucleobase mimetic would include more complicated structures, such as for example a tricyclic phenoxazine nucleobase mimetic. Methods for preparation of the above noted modified nucleobases are well known to those skilled in the art.
- oligomeric compounds provided herein comprise one or more nucleosides having a modified sugar moiety.
- the furanosyl sugar ring of a natural nucleoside can be modified in a number of ways including, but not limited to, addition of a substituent group, bridging of two non-geminal ring atoms to form a bicyclic nucleic acid (BNA) and substitution of an atom or group such as -S-, -N(R)- or -C(R 1 )(R 2 ) for the ring oxygen at the 4'-position.
- BNA bicyclic nucleic acid
- Modified sugar moieties are well known and can be used to alter, typically increase, the affinity of the antisense compound for its target and/or increase nuclease resistance.
- a representative list of modified sugars includes but is not limited to non-bicyclic substituted sugars, especially non-bicyclic 2'-substituted sugars having a 2'-F, 2'-OCH 3 or a 2'-O(CH 2 ) 2 -OCH 3 substituent group; and 4'-thio modified sugars.
- Sugars can also be replaced with sugar mimetic groups among others. Methods for the preparations of modified sugars are well known to those skilled in the art. Some representative patents and publications that teach the preparation of such modified sugars include, but are not limited to, U.S.
- Patents 4,981,957 ; 5,118,800 ; 5,319,080 ; 5,359,044 ; 5,393,878 ; 5,446,137 ; 5,466,786 ; 5,514,785 ; 5,519,134 ; 5,567,811 ; 5,576,427 ; 5,591,722 ; 5,597,909 ; 5,610,300 ; 5,627,053 ; 5,639,873 ; 5,646,265 ; 5,658,873 ; 5,670,633 ; 5,792,747 ; 5,700,920 ; and 6,600,032 ; and WO 2005/121371 .
- nucleosides comprise bicyclic modified sugars (BNA's), including LNA (4'-(CH 2 )-O-2' bridge), 2'-thio-LNA (4'-(CH 2 )-S-2' bridge),, 2'-amino-LNA (4'-(CH 2 )-NR-2' bridge)" ENA (4'-(CH 2 ) 2 -O-2' bridge), 4'-(CH 2 ) 3 -2' bridged BNA, 4'-(CH 2 CH(CH 3 ))-2' bridged BNA” cEt (4'-(CH(CH 3 )-O-2' bridge), and cMOE BNAs (4'-(CH(CH 2 OCH 3 )-O-2' bridge).
- BNA's bicyclic modified sugars
- LNAs Locked Nucleic Acids
- the 2'-hydroxyl group of the ribosyl sugar ring is linked to the 4' carbon atom of the sugar ring thereby forming a 2'-C,4'-C-oxymethylene linkage to form the bicyclic sugar moiety
- Patents: 6,268,490 and 6,670,461 The linkage can be a methylene (-CH 2 -) group bridging the 2' oxygen atom and the 4' carbon atom, for which the term LNA is used for the bicyclic moiety; in the case of an ethylene group in this position, the term ENATM is used ( Singh et al., Chem. Commun., 1998, 4, 455-456 ; ENATM: Morita et al.. Bioorganic Medicinal Chemistry, 2003, 11, 2211-2226 ).
- Tm +3 to +10° C
- Potent and nontoxic antisense oligonucleotides containing LNAs have been described ( Wahlestedt et al., Proc. Natl. Acad. Sci. U.S.A., 2000, 97, 5633-5638 ).
- alpha-L-LNA An isomer of LNA that has also been studied is alpha-L-LNA which has been shown to have superior stability against a 3'-exonuclease.
- the alpha-L-LNA's were incorporated into antisense gapmers and chimeras that showed potent antisense activity ( Frieden et al., Nucleic Acids Research, 2003, 21, 6365-6372 ).
- LNA monomers adenine, cytosine, guanine, 5-methyl-cytosine, thymine and uracil, along with their oligomerization, and nucleic acid recognition properties have been described ( Koshkin et al., Tetrahedron, 1998, 54, 3607-3630 ). LNAs and preparation thereof are also described in WO 98/39352 and WO 99/14226 .
- internucleoside linking groups that link the nucleosides or otherwise modified monomer units together thereby forming an antisense compound.
- the two main classes of internucleoside linking groups are defined by the presence or absence of a phosphorus atom.
- Representative phosphorus containing internucleoside linkages include, but are not limited to, phosphodiesters, phosphotriesters, methylphosphonates, phosphoramidate, and phosphorothioates.
- Non-phosphorus containing internucleoside linking groups include, but are not limited to, methylenemethylimino (-CH 2 -N(CH 3 )-O-CH 2 -), thiodiester (-O-C(O)-S-), thionocarbamate (-O-C(O)(NH)-S-); siloxane (-O-Si(H)2-O-); and N,N'-dimethylhydrazine (-CH 2 -N(CH 3 )-N(CH 3 )-).
- Antisense compounds having non-phosphorus internucleoside linking groups are referred to as oligonucleosides.
- Modified internucleoside linkages can be used to alter, typically increase, nuclease resistance of the antisense compound.
- Internucleoside linkages having a chiral atom can be prepared racemic, chiral, or as a mixture.
- Representative chiral internucleoside linkages include, but are not limited to, alkylphosphonates and phosphorothioates. Methods of preparation of phosphorous-containing and non-phosphorous-containing linkages are well known to those skilled in the art.
- a phosphate group can be linked to the 2', 3' or 5' hydroxyl moiety of the sugar.
- the phosphate groups covalently link adjacent nucleosides to one another to form a linear polymeric compound.
- the phosphate groups are commonly referred to as forming the internucleoside backbone of the oligonucleotide.
- the normal linkage or backbone of RNA and DNA is a 3' to 5' phosphodiester linkage.
- Oligomeric compounds comprise a 5' wing and a 3' wing.
- the features of the 3' wing and the features of the 5' wing are selected independently.
- the number of nucleosides in the 5' wing and the number of nucleosides (length) in the 3' wing may be the same or may be different;
- the modifications, if any, in the 5' wing may be the same as the modifications, if any, in the 3' wing or such modifications, if any, may be different;
- the internucleoside linkages in the 5' wing and the internucleoside linkages in the 3' wing may be the same or they may be different.
- a wing comprises one, two, three, four, or five nucleosides (i.e. has a length of 1, 2, 3, 4, or 5).
- the nucleosides of the wing are modified to increase affinity of the antisense compound for its target nucleic acid.
- the nucleosides of a wing are nucleosides or nucleotides.
- the nucleosides or nucleotides of the wing comprise a 2' modification.
- the nucleosides (nucleosides or nucleotides) of the wing are BNA's.
- the nucleosides of the wing are selected from ⁇ -L-Methyleneoxy (4'-CH,-O-2') BNA, ⁇ -D-Methyteneoxy (4'-CH 2 -O-2') BNA , Ethyleneoxy (4'-(CH 2 ) 2 -O-2') BNA , Aminooxy (4'-CH 2 -O-N(R)-2') BNA and Oxyamino(4'-CH 2 -N(R)-O-2') BNA.
- each R m and R n is, independently, H or substituted or unsubstituted C 1 -C 10 alkyl.
- the nucleosides of a wing are 2'MOE nucleotides.
- a wing comprises two, three, four, or five nucleosides
- those two, three, four, or five nucleosides are each selected independently.
- those two, three, four, or five nucleosides all comprise the same modifications, if any.
- one or more of those two, three, four, or five nucleobases comprises one or more modifications that is different from one or more of the modifications of one or more of the remaining nucleosides.
- one or more nucleoside of a 5' wing is different from at least one other nucleoside of the 5' wing.
- one or more nucleoside of a 3' wing is different from at least one other nucleoside of the 3' wing.
- one or more nucleoside of a 5' wing is different from at least one nucleoside of a 3' wing.
- all of the nucleosides of a 5' wing is different from all of the nucleosides of a 3' wing.
- one or more internucleoside linkage of a 5' wing is different from at least one other internucleoside linkage of the 5' wing.
- one or more internucleoside linkage of a 3' wing is different from at least one other internucleoside linkage of the 3' wing.
- one or more internucleoside linkage of a 5' wing is different from at least one internucleoside linkage of the 3' wing.
- all of the internucleoside linkages of a 5' wing is different from all of the internucleoside linkages of the 3' wing.
- the invention provides gapmer compounds wherein at least one nucleoside of one wing is differently modified compared to at least one other nucleoside of the same wing.
- Such oligomeric compounds are referred to as mixed wing oligomeric compounds.
- the modifications (or no modification) of one or more nucleosides of the 3' wing are different from those of one or more other nucleosides of the 3' wing.
- Such oligomeric compounds may be referred to as 3' mixed wing gapmers.
- the modifications (or no modification) of one or more nucleosides of the 5' wing are different from those of one or more other nucleosides of the 5' wing.
- Such oligomeric compounds may be referred to as 5' mixed wing gapmers.
- the modifications (or no modification) of one or more nucleosides of the 3' wing are different from those of one or more other nucleosides of the 3' wing and the modifications (or no modification) of one or more nucleosides of the 5' wing are different from those of one or more other nucleosides of the 5' wing.
- Such oligomeric compounds may be referred to as 3', 5' mixed wing gapmers.
- the modifications and combination of modifications at the 3' wing and at the 5' end may be the same or they may be different.
- mixed wing compounds have desirable properties.
- Certain nucleoside modifications confer on the oligomeric compound a desirable property, for example increased affinity for a target or nuclease resistance, but also confer an undesirable property, for example increased toxicity.
- Incorporation of certain other nucleoside modifications results in oligomeric compounds with different profiles of properties.
- the wings of a mixed wing oligomeric compound comprise one or more nucleoside comprising a first modification that increases affinity of the oligomeric compound for a target nucleic acid compared to an oligomeric compound comprising unmodified nucleosides; and one or more nucleoside comprising a second modification that results in reduced toxicity compared to an oligomeric compound with wings comprising nucleosides that all comprise the first modification.
- an oligomeric compound comprises at least one wing comprising at least one MOE substituted nucleoside and at least one LNA.
- the at least one MOE substituted nucleoside and the at least one LNA are in the 3' wing.
- the at least one MOE substituted nucleoside and the at least one LNA are in the 5' wing.
- oligomeric compounds comprise asymetric wings.
- each of the nucleoside(s) of the 3' wing comprise the same modification (or no modification) and each of the nucleoside(s) of the 5' wing comprise the same modification (or no modification), but the modifications of the 5' wing and the 3' wing are different from one another.
- the oligomeric compounds comprise a gap between the 5' wing and the 3' wing.
- the gap comprises seven, eight, nine or ten nucleotides.
- the nucleotides of the gap are unmodified deoxyribonucleotides.
- gap modifications (if any) gap result in an antisense compound that, when bound to its target nucleic acid, supports cleavage by an RNase, including, but not limited to, RNase H.
- the deoxy gap region of the antisense oligonucleotide is between 7 and 10 nucleotides in length. In certain embodiments, the gap comprises at least 7 nucleosides. In certain embodiments, the gap comprises at least 8 nucleosides. In certain embodiments, the gap comprises at least 9 nucleosides. In certain embodiments, the gap comprises 10 nucleosides.
- the wings and the gaps discussed above may be selected and then combined in a variety of combinations to generate gapped oligomeric compounds, including, but not limited to, gapped antisense oligomeric compounds, and gapped antisense oligonucleotides.
- the features (length, modifications, linkages) of the 5' wing and the 3' wing may be selected independently of one another.
- the features of the gap include at least one difference in modification compared to the features of the 5' wing and at least one difference compared to the features of the 3' wing (i.e., there must be at least one difference in modification between neighboring regions to distinguish those neighboring regions from one another).
- the features of the gap may otherwise be selected independently.
- the present invention provides oligomeric compounds of any of a variety of ranges of lengths.
- the invention provides oligomeric compounds comprising oligonucleotides consisting of 9 to 10, 9 to 11, 9 to 12, 9 to 13, 9 to 14, 9 to 15, 9 to 16, 9 to 17, 9 to 18, 9 to 19, 9 to 20, 9 to 21, 9 to 22, 9 to 23, 9 to 24, 9 to 25, 9 to 26, 9 to 27, 9 to 28, 9 to 29, 9 to 30, 10 to 11, 10 to 12, 10 to 13, 10 to 14, 10 to 15, 10 to 16, 10 to 17, 10 to 18, 10 to 19, 10 to 20, 10 to 21, 10 to 22, 10 to 23, 10 to 24, 10 to 25, 10 to 26, 10 to 27, 10 to 28, 10 to 29, 10 to 30, 11 to 12, 11 to 13, 11 to 14, 11 to 15, 11 to 16, 11 to 17, 11 to 18, 11 to 19, 11 to 20, 11 to 21, 11 to 22, 11 to 23, 11 to 24, 11 to 25, 11 to 26, 11 to 27, 11 to 28, 11 to 29, 11 to 30, 12 to 13, 12 to 14, 12 to 15, 12 to 16, 12 to 17, 12 to 18, 12
- oligomeric compounds are mixed wing gapmers.
- one or both wings of oligomeric compounds comprise one or more non-bicyclic 2' substituted nucleoside and one or more BNA nucleoside.
- Motifs disclosed herein, encompassing some within the scope of the claims, include, but are not limited to:
- nucleosides such as certain BNA nucleosides, confer increased potency and/or activity on an oligomeric compound relative to other nucleosides, such as MOE, but also confer increased toxicity.
- oligomeric compounds comprising mixed wings have better potency than oligomeric compounds with uniform MOE wings and less toxicity than uniform BNA compounds.
- mixed wing oligomeric compounds have higher therapeutic indexes than either oligomeric compounds comprising uniform BNA wings or oligomeric compound comprising uniform MOE wings.
- the BNA is selected from ⁇ -L-LNA, ⁇ -D-LNA, ENA, Oxyamino BNA (2'-ON(CH 3 )-CH 2 -4') and Aminooxy BNA (2'-N(CH 3 )-O-CH 2 -4').
- such oligomeric compounds comprise mixed backbones.
- such oligomeric compounds comprises uniform backbones.
- at least one internucleoside linkage is a phosphorothioate.
- each internucleoside linkage is a phosphorothioate.
- oligomeric compounds are modified by covalent attachment of one or more conjugate groups.
- conjugate groups modify one or more properties of the attached oligomeric compound including but not limited to pharmacodynamic, pharmacokinetic, binding, absorption, cellular distribution, cellular uptake, charge and clearance.
- Conjugate groups are routinely used in the chemical arts and are linked directly or via an optional linking moiety or linking group to a parent compound such as an oligomeric compound.
- conjugate groups includes without limitation, intercalators, reporter molecules, polyamines, polyamides, polyethylene glycols, thioethers, polyethers, cholesterols, thiocholesterols, cholic acid moieties, folate, lipids, phospholipids, biotin, phenazine, phenanthridine, anthraquinone, adamantane, acridine, fluoresceins, rhodamines, coumarins and dyes.
- Certain conjugate groups amenable to the present invention include lipid moieties such as a cholesterol moiety ( Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553 ); cholic acid ( Manoharan et al., Bioorg. Med. Chem. Lett., 1994, 4, 1053 ); a thioether, e.g., hexyl-S-tritylthiol ( Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660, 306 ; Manoharan et al., Bioorg. Med. Chem.
- lipid moieties such as a cholesterol moiety ( Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553 ); cholic acid ( Manoharan et al., Bioorg. Med. Chem. Lett., 1994, 4, 1053 ); a
- Acids Res., 1990, 18, 3777 a polyamine or a polyethylene glycol chain ( Manoharan et al., Nucleosides & Nucleotides, 1995, 14, 969 ); adamantane acetic acid ( Manoharan et al., Tetrahedron Lett., 1995, 36, 3651 ); a palmityl moiety ( Mishra et al., Biochim. Biophys. Acta, 1995, 1264, 229 ); or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety ( Crooke et al., J. Pharmacol. Exp. Ther., 1996,277,923 ).
- Linking groups or bifunctional linking moieties such as those known in the art are amenable to the compounds provided herein. Linking groups are useful for attachment of chemical functional groups, conjugate groups, reporter groups and other groups to selective sites in a parent compound such as for example an oligomeric compound.
- a bifunctional linking moiety comprises a hydrocarbyl moiety having two functional groups. One of the functional groups is selected to bind to a parent molecule or compound of interest and the other is selected to bind essentially any selected group such as chemical functional group or a conjugate group.
- the linker comprises a chain structure or an oligomer of repeating units such as ethylene glycol or amino acid units.
- bifunctional linking moieties include amino, hydroxyl, carboxylic acid, thiol, unsaturations (e.g., double or triple bonds), and the like.
- bifunctional linking moieties include 8-amino-3,6-dioxaoctanoic acid (ADO), succinimidyl 4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC) and 6-aminohexanoic acid (AHEX or AHA).
- linking groups include, but are not limited to, substituted C 1 -C 10 alkyl, substituted or unsubstituted C 2 -C 10 alkenyl or substituted or unsubstituted C 2 -C 10 alkynyl, wherein a nonlimiting list of preferred substituent groups includes hydroxyl, amino, alkoxy, carboxy, benzyl, phenyl, nitro, thiol, thioalkoxy, halogen, alkyl, aryl, alkenyl and alkynyl.
- the invention provides oligomeric compounds that are antisense compounds.
- Antisense mechanisms are all those involving the hybridization of a compound with target nucleic acid, wherein the outcome or effect of the hybridization is either target degradation or target occupancy with concomitant stalling of the cellular machinery involving, for example, transcription or splicing.
- compounds of the invention exert a biological effect through RNase H, which is a cellular endonuclease that cleaves the RNA strand of an RNA:DNA duplex.
- RNase H is a cellular endonuclease that cleaves the RNA strand of an RNA:DNA duplex.
- RNase H single-stranded antisense compounds which are "DNA-like" elicit RNAse H.
- Activation of RNase H therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of DNA-like oligonucleotide-mediated inhibition of gene expression.
- gapmers are capable of eliciting RNase H cleavage provided the gap is DNA-like and at least 4 nucleotides in length.
- the invention provides oligomeric compounds that are complementary to a target nucleic acid.
- targeting or “targeted to” refer to the process of designing an oligomeric compound such that the compound specifically hybridizes with a selected nucleic acid molecule.
- Targeting an oligomeric compound to a particular target nucleic acid molecule can be a multistep process. The process usually begins with the identification of a target nucleic acid whose expression is to be modulated.
- target nucleic acid and “nucleic acid encoding a target gene” encompass DNA encoding a selected target gene, RNA (including pre-mRNA and mRNA) transcribed from such DNA, and also cDNA derived from such RNA.
- the target nucleic acid can be a cellular gene (or mRNA transcribed from the gene) whose expression is associated with a particular disorder or disease state, or a nucleic acid molecule from an infectious agent.
- One of skill in the art will be able to design, synthesize, and screen oligomeric compounds of different nucleobase sequences to identify a sequence that results in antisense activity. For example, one may design an oligomeric compound that inhibits expression of a target protein. Methods for designing, synthesizing and screening oligomeric compounds for antisense activity against a preselected target nucleic acid can be found, for example in and " Antisense Drug Technology, Principles, Strategies, and Applications” Edited by Stanley T, Crooke, CRC Press, Boca Raton, Florida .
- antisense compounds that may contain up to about 20% nucleotides that disrupt base pairing of the antisense compound to the target. Preferably the compounds contain no more than about 15%, more preferably not more than about 10%, most preferably not more than 5% or no mismatches. The remaining nucleotides do not disrupt hybridization (e.g., universal bases).
- the compounds provided herein are at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% complementary to a target nucleic acid.
- Percent complementarity of an oligonucleotide is calculated by dividing the number of complementary nucleobases by the total number of nucleobases of the oligonucleotide. Percent complementarity of a region of an oligonucleotide is calculated by dividing the number of complementary nucleobases in the region by the total number of nucleobases region.
- T m melting temperature
- T m or ⁇ T m can be calculated by techniques that are familiar to one of ordinary skill in the art. For example, techniques described in Freier et al. (Nucleic Acids Research, 1997, 25, 22: 4429-4443 ) allow one of ordinary skill in the art to evaluate nucleotide modifications for their ability to increase the melting temperature of an RNA:DNA duplex.
- Antisense compounds, or a portion thereof, may have a defined percent identity to a SEQ ID NO, or a compound having a specific Isis number.
- a sequence is identical to the sequence disclosed herein if it has the same nucleobase pairing ability.
- a RNA which contains uracil in place of thymidine in the disclosed sequences of the compounds described herein would be considered identical as they both pair with adenine.
- This identity may be over the entire length of the oligomeric compound, or in a portion of the antisense compound (e.g., nucleobases 1-20 of a 27-mer may be compared to a 20-mer to determine percent identity of the oligomeric compound to the SEQ ID NO.) It is understood by those skilled in the art that an antisense compound need not have an identical sequence to those described herein to function similarly to the antisense compound described herein. Shortened versions of antisense compounds taught herein, or non-identical versions of the antisense compounds taught herein are also provided herein. Non-identical versions are those wherein each base does not have the same pairing activity as the antisense compounds disclosed herein.
- Bases do not have the same pairing activity by being shorter or having at least one abasic site.
- a non-identical version can include at least one base replaced with a different base with different pairing activity (e.g., G can be replaced by C, A, or T). Percent identity is calculated according to the number of bases that have identical base pairing corresponding to the SEQ ID NO or antisense compound to which it is being compared.
- the non-identical bases may be adjacent to each other, dispersed through out the oligonucleotide, or both.
- a 16-mer having the same sequence as nucleobases 2-17 of a 20-mer is 80% identical to the 20-mer.
- a 20-mer containing four nucleobases not identical to the 20-mer is also 80% identical to the 20-mer.
- a 14-mer having the same sequence as nucleobases 1-14 of an 18-mer is 78% identical to the 18-mer.
- the percent identity is based on the percent of nucleobases in the original sequence present in a portion of the modified sequence. Therefore, a 30 nucleobase antisense compound comprising the full sequence of the complement of a 20 nucleobase active target segment would have a portion of 100% identity with the complement of the 20 nucleobase active target segment, while further comprising an additional 10 nucleobase portion.
- the complement of an active target segment may constitute a single portion.
- the oligonucleotides provided herein are at least 80%, at least 85%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or 100% identical to at least a portion of the complement of the active target segments presented herein.
- Percent identity of an oligonucleotide is calculated by dividing the number of identical nucleobases by the total number of nucleobases of the oligonucleotide.
- Percent identity of a region of an oligonucleotide is calculated by dividing the number of identity nucleobases in the region by the total number of nucleobases region.
- provided herein are compounds having reactive phosphorus groups useful for forming internucleoside linkages including for example phosphodiester and phosphorothioate internucleoside linkages.
- Methods of preparation and/or purification of precursors or antisense compounds are not a limitation of the compositions or methods provided herein. Methods for synthesis and purification of DNA, RNA, and the antisense compounds are well known to those skilled in the art.
- Oligomerization of modified and unmodified nucleosides can be routinely performed according to literature procedures for DNA ( Protocols for Oligonucleotides and Analogs, Ed. Agrawal (1993), Humana Press ) and/or RNA ( Scaringe, Methods (2001), 23, 206-217 . Gait et al., Applications of Chemically synthesized RNA in RNA: Protein Interactions, Ed. Smith (1998), 1-36 . Gallo et al., Tetrahedron (2001), 57, 5707-5713 ).
- Antisense compounds provided herein can be conveniently and routinely made through the well-known technique of solid phase synthesis.
- Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems (Foster City, CA). Any other means for such synthesis known in the art may additionally or alternatively be employed. It is well known to use similar techniques to prepare oligonucleotides such as the phosphorothioates and alkylated derivatives.
- Analysis methods include capillary electrophoresis (CE) and electrospray-mass spectroscopy. Such synthesis and analysis methods can be performed in multi-well plates.
- CE capillary electrophoresis
- electrospray-mass spectroscopy Such synthesis and analysis methods can be performed in multi-well plates.
- the antisense compounds provided herein comprise any pharmaceutically acceptable salts, esters, or salts of such esters, or any other functional chemical equivalent which, upon administration to an animal including a human, is capable of providing (directly or indirectly) the biologically active metabolite or residue thereof. Accordingly, for example, the disclosure is also drawn to prodrugs and pharmaceutically acceptable salts of the antisense compounds, pharmaceutically acceptable salts of such prodrugs, and other bioequivalents.
- prodrug indicates a therapeutic agent that is prepared in an inactive or less active form that is converted to an active form (i.e., drug) within the body or cells thereof by the action of endogenous enzymes, chemicals, and/or conditions.
- prodrug versions of the oligonucleotides are prepared as SATE ((S-acetyl-2-thioethyl) phosphate) derivatives according to the methods disclosed in WO 93/24510 or WO 94/26764 .
- Prodrugs can also include antisense compounds wherein one or both ends comprise nucleobases that are cleaved (e.g., by incorporating phosphodiester backbone linkages at the ends) to produce the active compound. nucleobases that are cleaved (e.g., by incorporating phosphodiester backbone linkages at the ends) to produce the active compound.
- pharmaceutically acceptable salts refers to physiologically and pharmaceutically acceptable salts of the compounds described herein: i.e., salts that retain the desired biological activity of the parent compound and do not impart undesired toxicological effects thereto.
- Sodium salts of antisense oligonucleotides are useful and are well accepted for therapeutic administration to humans.
- sodium salts of dsRNA compounds are also provided.
- antisense compounds provided herein may also be admixed, encapsulated, conjugated or otherwise associated with other molecules, molecule structures or mixtures of compounds.
- compositions and formulations which include the antisense compounds provided herein.
- the pharmaceutical compositions may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated.
- administration is topical to the surface of the respiratory tract, particularly pulmonary, e.g., by nebulization, inhalation, or insufflation of powders or aerosols, by mouth and/or nose.
- compositions described herein may be prepared according to conventional techniques well known in the pharmaceutical industry. Such techniques include the step of bringing into association the active ingredients with the pharmaceutical carrier(s) or excipient(s). In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers, finely divided solid carriers, or both, and then, if necessary, shaping the product (e.g., into a specific particle size for delivery).
- the pharmaceutical formulations are prepared for pulmonary administration in an appropriate solvent, e.g., water or normal saline, possibly in a sterile formulation, with carriers or other agents to allow for the formation of droplets of the desired diameter for delivery using inhalers, nasal delivery devices, nebulizers, and other devices for pulmonary delivery.
- an appropriate solvent e.g., water or normal saline
- the pharmaceutical formulations may be formulated as dry powders for use in dry powder inhalers.
- a “pharmaceutical carrier” or “excipient” can be a pharmaceutically acceptable solvent, suspending agent or any other pharmacologically inert vehicle for delivering one or more nucleic acids to an animal and are known in the art.
- the excipient may be liquid or solid and is selected, with the planned manner of administration in mind, so as to provide for the desired bulk, consistency, etc., when combined with a nucleic acid and the other components of a given pharmaceutical composition.
- compositions provided herein can contain two or more antisense compounds.
- compositions can contain one or more antisense compounds, particularly oligonucleotides, targeted to a first nucleic acid and one or more additional antisense compounds targeted to a second nucleic acid target.
- compositions can contain two or more antisense compounds targeted to different regions of the same nucleic acid target. Two or more combined compounds may be used together or sequentially.
- Compositions can also be combined with other non-antisense compound therapeutic agents.
- antisense compounds provided herein can be utilized for diagnostics, and as research reagents and kits. Furthermore, antisense compounds, which are able to inhibit gene expression or modulate gene expression with specificity, are often used by those of ordinary skill to elucidate the function of particular genes or to distinguish between functions of various members of a biological pathway.
- the antisense compounds described herein can be used as tools in differential and/or combinatorial analyses to elucidate expression patterns of a portion or the entire complement of genes expressed within cells and tissues. Methods of gene expression analysis are well known to those skilled in the art.
- Antisense compounds provided herein can be used to modulate the expression of a target gene in an animal, such as a human.
- the provided compounds also can be used to treat metabolic disorders or modulate one or more disease indications.
- the methods comprise the step of administering to said animal in need of therapy for a disease or condition associated with a target gene an effective amount of an antisense compound that modulates expression of the target gene.
- Antisense compounds provided herein which effectively modulate expression of a target RNA or protein products of expression are considered active antisense compounds.
- Active antisense compounds also include compounds which effectively modulate one or more of a number of disease indications, including metabolic and cardiovascular disease indications, examples of which are described below.
- Modulation of expression of a target gene can be measured in a bodily fluid, which may or may not contain cells: tissue; or organ of the animal.
- tissue which may or may not contain cells: tissue; or organ of the animal.
- samples for analysis such as body fluids (e.g., sputum, serum, urine), tissues (e.g., biopsy), or organs, and methods of preparation of the samples to allow for analysis are well known to those skilled in the art.
- Methods for analysis of RNA and protein levels are discussed above and are well known to those skilled in the art.
- the effects of treatment can be assessed by measuring biomarkers, or disease indications, associated with the target gene expression in the aforementioned fluids, tissues or organs, collected from an animal contacted with one or more compounds described herein, by routine clinical methods known in the art.
- biomarkers include but are not limited to: liver transaminases, bilirubin, albumin, blood urea nitrogen, creatine and other markers of kidney and liver function; interleukins, tumor necrosis factors, intracellular adhesion molecules, C-reactive protein, chemokines, cytokines, and other markers of inflammation.
- the antisense compounds provided herein can be utilized in pharmaceutical compositions by adding an effective amount of a compound to a suitable pharmaceutically acceptable diluent or carrier.
- Acceptable carriers and diluents are well known to those skilled in the art. Selection of a diluent or carrier is based on a number of factors, including, but not limited to, the solubility of the compound and the route of administration. Such considerations are well understood by those skilled in the art.
- the antisense compounds described herein inhibit expression of a target gene.
- the compounds can also be used in the manufacture of a medicament for the treatment of diseases and disorders related to a target gene.
- Bodily fluids, organs or tissues can be contacted with one or more of the compounds resulting in modulation of target gene expression in the cells of bodily fluids, organs or tissues.
- An effective amount can be determined by monitoring the modulatory effect of the antisense compound or compounds or compositions on target nucleic acids or their products by methods routine to the skilled artisan.
- nucleoside modifications and conjugate groups The sequences listed in the examples have been annotated to indicate the location and type of nucleoside modifications and conjugate groups. All of the nucleosides that are not annotated are ⁇ -D-deoxyribonudeosides. Each modified nucleoside is preceded by a subscripted letter or a letter followed by a number wherein the letter indicates the type of modification and the number indicates a further modification at a particular position.
- subscript "m” indicates a 2'-O-methyl group
- subscript "1” indicates a bicyclic nucleoside having a 4'-CH 2 -O-2' bridge, also referred to as LNA
- subscript "g” indicates a bicyclic nucleoside having a 4'-(CH 2 ) 2 -O-2' bridge, also referred to as ENA
- subscript "#1" (# is 5 or 6) indicates a bicyclic nucleoside having a 4'-CH 2 -O-2' bridge (LNA) having a further substituent group located at the 5' or 6' position of the bicyclic nucleoside which can also be chiral (R) or (S)
- subscript "e” indicates 2'-O-methoxyethyl (MOE) group
- U e is a modified uridine having a 2'-O-methoxyethyl group and U 51 is an LNA modified uridine having a further substituent at the 5'-position.
- sequence listing accompanying this filing provides certain nucleic acid sequences independent of chemical modification. Though that listing identifies each sequence as either "RNA” or "DNA” as required, those sequences may be modified with any combination of chemical modifications and/or motifs.
- oligomeric compounds on target nucleic acid expression can be tested in any one of a number of cultured or primary cell lines.
- Cells lines can be obtained from publicly available sources, such as the American Type Culture Collection (Manassas, VA). Cells are cultured according to methods well known to those of ordinary skill in the art.
- oligonucleotide When cells reached appropriate confluency, they were treated with oligonucleotide using LipofectinTM as described. When cells reached 65-75% confluency, they were treated with oligonucleotide. Oligonucleotide was mixed with LIPOFECTINTM Invitrogen Life Technologies, Carlsbad, CA) in Opti-MEMTM-1 reduced serum medium (Invitrogen Life Technologies, Carlsbad, CA) to achieve the desired concentration of oligonucleotide and a LIPOFECTINTM concentration of 2.5 or 3 ⁇ g/mL per 100 nM oligonucleotide. This transfection mixture was incubated at room temperature for approximately 0.5 hours.
- OPTI-MEMTM-1 For cells grown in 96-well plates, wells were washed once with 100 ⁇ L OPTI-MEMTM-1 and then treated with 130 ⁇ L of the transfection mixture. Cells grown in 24-well plates or other standard tissue culture plates were treated similarly, using appropriate volumes of medium and oligonucleotide. Cells were treated and data were obtained in duplicate or triplicate. After approximately 4-7 hours of treatment at 37°C, the medium containing the transfection mixture was replaced with fresh culture medium. Cells were harvested 16-24 hours after oligonucleotide treatment.
- Control oligonucleotides are used to determine the optimal oligomeric compound concentration for a particular cell line. Furthermore, when oligomeric compounds are tested in oligomeric compound screening experiments or phenotypic assays, control oligonucleotides are tested in parallel.
- the concentration of oligonucleotide used varies from cell line to cell line. To determine the optimal oligonucleotide concentration for a particular cell line, the cells are treated with a positive control oligonucleotide at a range of concentrations. The concentration of positive control oligonucleotide that results in 80% inhibition of the target mRNA is then utilized as the screening concentration for new oligonucleotides in subsequent experiments for that cell line. If 80% inhibition is not achieved, the lowest concentration of positive control oligonucleotide that results in 60% inhibition of the target mRNA is then utilized as the oligonucleotide screening concentration in subsequent experiments for that cell line.
- concentrations of antisense oligonucleotides used herein are from 50 nM to 300 nM when the antisense oligonucleotide is transfected using a liposome reagent 1 ⁇ M to 40 ⁇ M when the antisense oligonucleotide is transfected by electroporation.
- Quantitation of target mRNA levels was accomplished by real-time quantitative PCR using the ABI PRISMTM 7600, 7700, or 7900 Sequence Detection System (PE-Applied Biosystems, Foster City, CA) according to manufacturer's instructions.
- RNA Prior to quantitative PCR analysis, primer-probe sets specific to the target gene being measured were evaluated for their ability to be "multiplexed" with a GAPDH amplification reaction. After isolation the RNA is subjected to sequential reverse transcriptase (RT) reaction and real-time PCR, both of which are performed in the same well.
- RT and PCR reagents were obtained from Invitrogen Life Technologies (Carlsbad, CA).
- RT real-time PCR was carried out in the same by adding 20 ⁇ L PCR cocktail (2.5x PCR buffer minus MgCl 2 , 6.6 mM MgCl 2 , 375 ⁇ M each of dATP, dCTP, dCTP and dGTP, 375 nM each of forward primer and reverse primer, 125 nM of probe, 4 Units RNAse inhibitor, 1.25 Units PLATINUM® Taq, 5 Units MuLV reverse transcriptase, and 2.5x ROX dye) to 96-well plates containing 30 ⁇ L total RNA solution (20-200 ng). The RT reaction was carried out by incubation for 30 minutes at 48°C.
- PCR cocktail 2.5x PCR buffer minus MgCl 2 , 6.6 mM MgCl 2 , 375 ⁇ M each of dATP, dCTP, dCTP and dGTP, 375 nM each of forward primer and reverse primer, 125 nM of probe, 4
- Gene target quantities obtained by RT, real-time PCR were normalized using either the expression level of GAPDH, a gene whose expression is constant, or by quantifying total RNA using RiboGreen TM (Molecular Probes, Inc. Eugene, OR).
- GAPDH expression was quantified by RT, real-time PCR, by being run simultaneously with the target, multiplexing, or separately.
- Total RNA was quantified using RiboGreen TM RNA quantification reagent (Molecular Probes, Inc. Eugene, OR).
- RiboGreen TM working reagent 170 ⁇ L of RiboGreen TM working reagent (RiboGreen TM reagent diluted 1:350 in 10mM Tris-HCl, 1 mM EDTA, pH 7.5) was pipetted into a 96-well plate containing 30 ⁇ L purified cellular RNA. The plate was read in a CytoFluor 4000 (PE Applied Biosystems) with excitation at 485nm and emission at 530nm.
- the GAPDH PCR probes have JOE covalently linked to the 5' end and TAMRA or MGB covalently linked to the 3' end, where JOE is the fluorescent reporter dye and TAMRA or MGB is the quencher dye.
- primers and probe designed to a GAPDH sequence from a different species are used to measure GAPDH expression.
- a human GAPDH primer and probe set is used to measure GAPDH expression in monkey-derived cells and cell lines.
- Probes and primers for use in real-time PCR were designed to hybridize to target-specific sequences. Primer and probe sequences and target genes to which they hybridize are presented in Table 1.
- the target-specific PCR probes have FAM covalently linked to the 5' end and TAMRA or MGB covalently linked to the 3' end, where FAM is the fluorescent dye and TAMRA or MGB is the quencher dye.
- mice Male 6-week old Balb/c mice (Jackson Laboratory, Bar Harbor, ME) were given a single 8 ⁇ mol/kg intraperitoneal injection of a PTEN antisense oligonucleotide (ASO) from Table 3. Mice were sacrificed 72 hours following ASO or control (saline) injection and serum concentrations of liver transaminases (alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) measured in international units (IU)/L as indicators of liver damage, using methods well-known by those of ordinary skill in the art.
- Target (PTEN) mRNA levels in the liver were determined by methods well-known by those of ordinary skill in the art, and reduction in target mRNA listed as percent of untreated control (% UTC).
- the gapmer antisense oligonucleotides having 2'-MOE nucleotides added to either of the 3' and the 5' wing regions resulted in a mitigation of the elevated serum transaminases caused by the LNA gapmer, ISIS 392056.
- Gapmers with 2'-MOE modification of only the 5' wings (one or both nucleotides) of LNA-modified antisense oligonucleotides resulted in serum transaminase concentrations near that of the 2'MOE gapmer antisense oligonucleotide (ISIS 394424) following administration to mice, indicating that substitution of specific LNA nucleoside(s) with 2'-modified nucleoside(s) provided a compound with an improved hepatotoxicity profile. These compounds also reduced target PTEN mRNA relative to the UTC.
- each compound is targeted to published ApoB sequences including Genbank Accession No. U92437.1 (SEQ ID NO: 7), (site 140).
- Each compound is a 2-10-2 gapmer (shortmer), which is 14 nuclcotides in length having a central "gap" region consisting often 2'-deoxynucleotides that is flanked by a 5' and a 3' "wing" region, each 2 nucleotides in length.
- wing nucleotides of the individual ASO compounds bear distinct sugar modifications.
- Each compound included a 5' terminal C16-G having the following structure: Table 4 Short Antisense Compounds with wing modifications ISIS # Sequence SEQ ID NO 391871 C l6 -GG 6 TACATGGAAGT e C e 9 391872 C l6 -GG l TACATGGAAGT l C l 9
- mice Male 6-week old Balb/c mice (Jackson Laboratory, Bar Harbor, ME) were administered twice per week for three weeks a single dose of a ApoB antisense oligonucleotide (ASO) from Table 5 by intraperitoneal injection at a concentration of 2.5, 1.0, 0.4 or 0.16 ⁇ mol/kg.
- Mice were sacrificed 48 hours following last administraton of ASO or control (saline) injection and serum concentrations of liver transaminases (alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) measured in international units (IU)/L, and bilirubin, free cholesterol, triglycerides, HDL and LDL, measured in international units mg/L.
- IU international units
- bilirubin free cholesterol, triglycerides, HDL and LDL, measured in international units mg/L.
- Target (ApoB) mRNA levels in the liver were determined by methods well-known by those of ordinary skill in the art, and reduction in target mRNA listed as percent of untreated control (% UTC). As illustrated in Table 5, ApoB mRNA levels were reduced in a dose-dependent manner. Table 5 Target mRNA Reduction Following Administration of LNA-Modified and 2'-MOE modified Antisense Oligonucleotides ISIS # Dose ( ⁇ mol/kg) ApoB mRNA (% UTC) Wing Chemistry saline 100.0 N/A 391871 0.16 105 2'-MOE wings w/ C 16 at 5'pos. 1 0.4 95 1.0 82 2.5 51 391872 0.16 98 LNA wings w/ C 16 at 5' pos. 1 0.4 50 1.0 8 2.5 0.8
- Plasma concentrations of total cholesterol, free cholesterol, triglycerides, transaminases, bilirubin, LDL and HDL were measured according to routine experimental procedures. The results are summarized in Table 6 below.
- Table 6 Liver Transaminases, Bilirubin levels, Cholesterol levels, Triglycerides levels, HDL and LDL levels Following Administration of LNA-Modified and 2'-MOE modified Antisense Oligonucleotides ISIS # Dose ALT AST Bilirubin Cholesterol HDL Triglycerides LDL 391871 0.16 38 95 0.175 106 78 253 8.0 0.4 40 98 0.150 109 79 256 8.0 1 32 44 0.175 108 82 219 6.8 2.5 38 133 0.150 90 65 236 5.5 391872 0.16 31 55 0.175 101 78 212 6.8 0.4 30 78 0.150 77 58 220 4.3 1 38 100 0.175 28 19 109 2.0 2.5 38 59 0.200 14 6 76
- liver, kidney and spleen were harvested from animals treated with the oligomeric compounds and were weighed to assess gross organ alterations. Approximateaverage tissue weights for each short antisense aompounds are presented in Table 7. Table 7 Effects of LNA-Modified and 2'-MOE modified Antisense Oligonucleotides Targeted to ApoB on Tissue Weight in Balb/c mice.
- liver weight spleen weight saline N/A 1.00 1.00 391871 0.16 0.92 (-8%) 0.97 (-3%) 0.4 0.98 (-2%) 1.02 (+2%) 1.0 0.97 (-3%) 0.99 (-1%) 2.5 1.08 (+8%) 1.12 (+12%) 391872 0.16 0.92 (-8%) 1.04 (+3%) 0.4 0.98 (-2%) 1.18 (+18%) 1.0 1.10 (+10%) 1.01 (+1%) 2.5 1.10 (+10%) 1:11 (+11%)
- Each compound is a 2-14-2 gapmer, which is 18 nucleotides in length having a central "gap" region consisting of forteen 2'-deoxynucleotides that is flanked by a 5' and a 3' "wing" region, each 2 nucleotides in length. As shown in Table 8, wing nucleotides of the individual ASO compounds bear distinct sugar modifications.
- mice Male 6-week old Balb/c mice (Jackson Laboratory, Bar Harbor, ME) were given a single 10 or 2 ⁇ mol/kg intraperitoneal injection of a PTEN antisense oligonucleotide (ASO) from Table 9. Mice were sacrificed 72 hours following ASO or control (saline) injection and serum concentrations of liver transaminases (alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) measured in international units (IU)/L as indicators of liver damage, using methods well-known by those of ordinary skill in the art.
- ASO PTEN antisense oligonucleotide
- Target (PTEN) mRNA levels in the liver were determined by methods well-known by those of ordinary skill in the art, and reduction in target mRNA listed as percent of untreated control (% UTC). The results are summarized in Table 9.
- Table 9 Liver Transaminases and Target mRNA Reduction Following Administration of LNA-Modified and 2'-MOE modified Antisense Oligonucleotides ISIS # Dose ( ⁇ mol/kg) ALT AST PTEN mRNA (% UTC) Wing Chemistry saline 39 66 100 N/A 394420 2 30 78 79 2'-MOE wings 10 49 91 26 394425 2 41 78 11 LNA wings 10 2453 2240 2 399700 2 45 148 36 LNA wings w/ a 2'-MOE at 5' pos.
- the gapmer antisense oligonucleotides having 2'-MOE nucleotides added to either of the 3' and the 5' wing regions resulted in a mitigation of the elevated serum transaminases caused by the LNA gapmer, ISIS 394425.
- Gapmers with 2'-MOE modification of only the 5' wings (one or both nucleotides) of LNA-modified antisense oligonucleotides resulted in serum transaminase concentrations near that of the 2'MOE gapmer antisense oligonucleotide (ISIS 394420) following administration to mice, indicating that substitution of specific LNA nucleoside(s) with 2'-modified nucleoside(s) provided a compound with an improved hepatotoxicity profile. These compounds also reduced target PTEN mRNA relative to the UTC.
- Gapmers with 2'-MOE modification of 3' wing resulted in a mitigation of the transaminase elevation caused by the LNA gapmer antisense oligonucleotide.
- ISIS 399703 both nucleotides
- 2'-MOE modification of wing nucleotides can mitigate hepatatoxicity of 2-14-2 LNA gapmers to levels which are commensurate with other 2'-MOE gapmers, while maintaining target mRNA reduction.
- the studies described herein were performed using a number of modified 1-9-2 gapmer oligonucleotides to determine whether nucleotide modification could mitigate hepatatoxicity associated with the locked nucleic acid (LNA) moiety.
- LNA locked nucleic acid
- the sequences and motifs of antisense compounds used in these studies are shown in Table 11. Each compound is targeted to published PTEN sequences including Genbank Accession No. U92437.1 (SEQ ID NO: 7), (site 140).
- Each compound is a 1-9-2 gapmer (shortmer), which is 12 nucleotides in length having a central "gap" region consisting of nine 2'-deoxynucleotides that is flanked by a 5' and a 3' "wing" region.
- the 5' wing region contains one nucleotide in length and the 3' wing region contains two nucleotides in length.
- wing nucleotides of the individual ASO compounds bear distinct sugar modifications.
- Table 11 Short LNA Antisense Compounds with MOE modifications ISIS # Sequence SEQ ID NO 396151 T e GGTCCAGAG me C e me C e 11 396153 T l GGTCCAGAG me C l me C l 11 401350 T e GGTCCAGAG me C l me C l 11 401349 T l GGTCCAGAG me C e me C e 11 401351 T a GGTCCAGAG me C l me C l 11 401352 C l6 -TGGTCCAGAG me C l me C l 11
- mice Male 6-week old Balb/c mice (Jackson Laboratory, Bar Harbor, ME) were given a single 10 or 3.2, 1, or 0.32 ⁇ mol/kg intraperitoneal injection of a PTEN antisense oligonucleotide (ASO) from Table 11. Mice were sacrificed 72 hours following ASO or control (saline) injection and serum concentrations of liver transaminases (alanine aminotransferase [ALT] and aspartate aminotransferase [AST]) measured in international units (IU)/L as indicators of liver damage, using methods well-known by those of ordinary skill in the art.
- ASO PTEN antisense oligonucleotide
- Target (PTEN) mRNA levels in the liver were determined by methods well-known by those of ordinary skill in the art, and reduction in target mRNA listed as percent of untreated control (% UTC). Results are summarized in Table 12.
- Table 12 Liver Transaminases and Target mRNA Reduction Following Administration of LNA-Modified and 2'-MOE modified Antisense Oligonucleotides ISIS # Dose ( ⁇ mol/kg) ALT AST PTEN mRNA (% UTC) Wing Chemistry saline N/A 39 66 100 N/A 396151 0.32 53 69 97 2'-MOE wings 1 53 98 3.2 64 97 71 10 89 101 23 396153 0.32 52 120 63 LNA wings 1 71 110 24 3.2 750 467 8 10 9681 4233 11 401350 0.32 55 105 80 1 61 125 49 2'-MOE at 5' wing 3.2 69 107 15 LNA at 3' wing 10 2183 1033 6 401349 0.32 67
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Claims (10)
- Gapmer-Antisense-Oligonukleotid, umfassend einen Desoxy-Zwischenraum("gap")-Bereich, einen am 5'-Ende des Desoxy-Zwischenraums liegenden 5'-endständigen ("5' wing"-)Bereich und einen am 3'-Ende des Desoxy-Zwischenraums liegenden 3'-endständigen ("3' wing"-)Bereich, wobei es sich bei wenigstens einem Nukleosid wenigstens eines der endständigen Bereiche um ein 4'-nach-2'-bicyclisches Nukleosid und bei wenigstens einem der restlichen Nukleoside des endständigen Bereichs um ein nicht-bicyclisches 2'-O(CH2)2OCH3-modifiziertes Nukleosid handelt, und wobei der Desoxy-Zwischenraum-Bereich eine Länge zwischen 7 und 10 Nukleotiden aufweist und die endständigen Bereiche eine Länge zwischen 1 und 7 Nukleosiden aufweisen und die oligomere Verbindung wenigstens eine modifizierte Internukleosidverknüpfung aufweist.
- Oligomere Verbindung nach Anspruch 1, wobei es sich bei dem 4'-nach-2'-bicyclischen Nukleosid um ein LNA-Nukleosid handelt.
- Oligomere Verbindung nach Anspruch 1, wobei es sich bei dem 4'-nach-2'-bicyclischen Nukleosid um ein methylenoxy(4'-CH2-O-2')-bicyclisches Nukleosid oder ethylenoxy (4'-CH2CH2-O-2') -bicyclisches Nukleosid handelt.
- Oligomere Verbindung nach einem der Ansprüche 1 bis 3, wobei die endständigen Bereiche eine Länge zwischen 1 und 3 Nukleosiden aufweisen.
- Oligomere Verbindung nach einem der Ansprüche 1 bis 4, wobei der 3'-endständige Bereich wenigstens ein 4'-nach-2'-bicyclisches Nukleosid umfasst.
- Oligomere Verbindung nach einem der Anspruch 5, wobei der 5'-endständige Bereich wenigstens ein nicht-bicyclisches 2'-O(CH2)2OCH3-modifiziertes Nukleosid umfasst.
- Oligomere Verbindung nach einem der Ansprüche 1 bis 4, wobei der 5'-endständige Bereich wenigstens ein 4'-nach-2'-bicyclisches Nukleosid aufweist.
- Oligomere Verbindung nach Anspruch 7, wobei der 3'-endständige Bereich wenigstens ein nicht-bicyclisches 2'-O(CH2)2OCH3-modifiziertes Nukleosid aufweist.
- Oligomere Verbindung nach einem der Ansprüche 1 bis 8, wobei es sich bei der modifizierten Internukleosidverknüpfung um ein Phosphorothioat handelt, wobei die oligomere Verbindung mehrere Phosphorothioat-Internukleosidverknüpfungen aufweist.
- Oligomere Verbindung nach einem der Ansprüche 1 bis 9 zur Verwendung bei einem therapeutischen Verfahren zur Verringerung der Expression einer Ziel-RNA bei einem Tier, wobei man bei dem Verfahren dem Tier das Gapmer-Antisense-Oligonukleotid verabreicht, wobei die Sequenz des Antisense-Oligonukleotids zur Ziel-RNA komplementär ist.
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